the Effect of Oral Vasopressors for Liberation From IV Vasopressors in

Clinical Trial Summary

the study is developed to evaluate the effect of use of oral vasopressors (midodrine versus minirin) on weaning ICU patients from IV vasopressors (noradrenaline) and compare between them for efficacy in shortage the duration of IV vasopressor and has low complications and side effects.

See also
	Status	Clinical Trial	Phase
	Recruiting	`NCT05637645` - Different Approaches of Spinal Anesthesia in Patients Undergoing Cesarean Section	N/A
	Withdrawn	`NCT05207826` - Detrusor Activity Recovery in Acute Traumatic Spinal Cord Injuries

See also

Status

Clinical Trial

Phase

Recruiting

NCT05637645 - Different Approaches of Spinal Anesthesia in Patients Undergoing Cesarean Section

N/A

Withdrawn

NCT05207826 - Detrusor Activity Recovery in Acute Traumatic Spinal Cord Injuries

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT04586790
Study type	Interventional
Source	Assiut University
Contact	Ahmed T Ahmed, lecture
Phone	01062716629
Email	Ahmedtalaat_ahmed@yahoo.com
Status	Recruiting
Phase	Phase 2
Start date	October 15, 2020
Completion date	January 28, 2021

the Effect of Oral Vasopressors for Liberation From IV Vasopressors in Spinal Shock

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms